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Related Concept Videos

Enzyme-Linked Immunosorbent Assay01:33

Enzyme-Linked Immunosorbent Assay

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In 1971, Peter Perlman and Eva Engvall developed an Enzyme-linked immunosorbent assay (ELISA or EIA). ELISA differs from western blot in that the assays are conducted in microtiter plates or in vivo rather than on an absorbent membrane.
There are many different types of ELISAs, but they all involve an antibody molecule whose constant region binds an enzyme, leaving the variable region free to bind its specific antigen.  Enzyme-substrate reaction allows the antigen to be visualized or...
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Development of a Lateral Flow Immunochromatographic Strip for Rapid and Quantitative Detection of Small Molecule Compounds
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Instrumentation-Free Semiquantitative Immunoanalysis Using a Specially Patterned Lateral Flow Assay Device.

Kyung Won Lee1, Ye Chan Yu1, Hyeong Jin Chun1

  • 1Department of Molecular Science and Technology, Ajou University, Suwon 16499, Korea.

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|August 6, 2020
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Summary

This study introduces a novel semi-quantitative lateral flow immunoassay (SQ-LFI) that uses colored spots for naked-eye quantification. This innovation eliminates the need for external equipment, enabling easy estimation of analyte concentration in resource-limited settings.

Keywords:
instrument-free quantitative analysislateral flow immunoassaymicroalbuminuriarenal failure

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Area of Science:

  • Biomedical Engineering
  • Analytical Chemistry
  • Immunodiagnostics

Background:

  • Traditional colorimetric lateral flow immunoassays (LFAs) using gold nanoparticles (AuNPs) require external equipment for signal quantification.
  • The single test line in conventional LFAs presents a limitation for naked-eye analysis.
  • There is a need for simple, equipment-free diagnostic tools, especially in resource-limited environments.

Purpose of the Study:

  • To develop a semi-quantitative lateral flow immunoassay (SQ-LFI) system for naked-eye quantification of analytes.
  • To eliminate the need for external optical instruments in LFA signal detection.
  • To demonstrate the utility of the SQ-LFI system in practical immunoassays.

Main Methods:

  • Modified the conventional LFA test zone into patterned spots forming herringbone patterns.
  • Utilized AuNPs as optical probes in a sandwich immunoassay format.
  • Quantified analyte concentration by counting the number of colored spots, correlating with analyte concentration.

Main Results:

  • The number of colored spots in the SQ-LFI system increased proportionally with analyte concentration.
  • Successfully analyzed microalbumin in artificial urine samples, with a detection range of 0–500 μg/mL.
  • Achieved a limit of detection (LOD) of 15.5 μg/mL for microalbumin.

Conclusions:

  • The developed SQ-LFI system enables naked-eye semi-quantification of analytes without external equipment.
  • This system is applicable for practical immunoanalysis, as demonstrated with microalbumin detection.
  • The SQ-LFI offers a promising solution for efficient, low-cost diagnostic devices in resource-limited settings.